AID* Kit
(Kit #
1000000120
)
Depositing Lab: Helle Ulrich
The AID* Kit is an expanded tool kit for the auxin-inducible degron (AID) system in budding yeast. By expanding the AID degron sequence to include tags for easy detection by antibodies/microscopy, and introducing a set of selection markers, this tool kit provides enhanced flexibility in applying the AID system by facilitating the detection of AID-tagged proteins, comparing their stability with those of untagged or endogenous proteins, and exerting a better control over initial protein levels.
This kit will be shipped as bacterial glycerol stocks in a 96-well plate format.
Original Publication
An expanded tool kit for the auxin-inducible degron system in budding yeast. M. Morawska & H.D. Ulrich Yeast. 2013 Sep 1;30(9):341-51. doi: 10.1002/yea.2967. PubMed PMID: 23836714.
Description
Fusion of inducible degradation signals, so-called degrons, to cellular proteins is an elegant method of controlling protein levels in vivo. In the budding yeast, Saccharomyces cerevisiae, this is most conveniently accomplished by a PCR-based tagging strategy where a degron tag is fused to the endogenous gene of interest.
The AID* tool kit for degron tagging in S. cerevisiae contains a set of vectors to be used as PCR templates for fusion of the “AID*” tag, expanded by a range of epitopes for ease of detection by commercial antibodies or fluorescence microscopy. The vectors are compatible with PCR-based genomic tagging strategies, allow for C- or N-terminal fusion of the degron, and provide a range of selection markers (kanMX, hphNT, natNT, HIS3MX). In addition, the kit includes vectors for expression of an F-box protein compatible with the yeast SCF ubiquitin ligase, which is required to induce degradation of the tagged protein upon addition of auxin. Induction of degradation is reversible and quick, measured in minutes rather than hours.
Protocols
Up-to-date information regarding this kit can be found at the Ulrich Lab website.
How to Cite this Kit
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which they were created, and include Addgene in the Materials and Methods of your future publications.
For your Materials and Methods section:
“The AID* Kit was a gift from Helle Ulrich (Addgene kit #1000000120).”
For your Reference section:
An expanded tool kit for the auxin-inducible degron system in budding yeast. M. Morawska & H.D. Ulrich Yeast. 2013 Sep 1;30(9):341-51. doi: 10.1002/yea.2967. PubMed PMID: 23836714.
AID* Kit - #1000000120
- Resistance Color Key
Each circle corresponds to a specific antibiotic resistance in the kit plate map wells.
- Inventory
Searchable and sortable table of all plasmids in kit. The Well column lists the plasmid well location in its plate. The Plasmid column links to a plasmid's individual web page.
- Kit Plate Map
96-well plate map for plasmid layout. Hovering over a well reveals the plasmid name, while clicking on a well opens the plasmid page.
Resistance Color Key
Ampicillin |
Inventory
Well | Plasmid | Resistance |
---|---|---|
A / 1 | pHyg-AID(1-114) | Ampicillin |
A / 2 | pHyg-AID(31-114) | Ampicillin |
A / 3 | pHyg-AID* | Ampicillin |
A / 4 | pHyg-AID(1-114)-8myc | Ampicillin |
A / 5 | pHyg-AID(31-114)-9myc | Ampicillin |
A / 6 | pHyg-AID*-9myc | Ampicillin |
A / 7 | pHyg-AID*-6FLAG | Ampicillin |
A / 8 | pHyg-AID*-6HA | Ampicillin |
A / 9 | pHyg-AID*-GFP | Ampicillin |
A / 10 | pKan-AID*-9myc | Ampicillin |
A / 11 | pNat-AID*-9myc | Ampicillin |
A / 12 | pHis-AID*-9myc | Ampicillin |
B / 1 | pKan-PCUP1-AID*(N) | Ampicillin |
B / 2 | pKan-PCUP1-AID*(N)-9myc | Ampicillin |
B / 3 | pKan-PCUP1-9myc-AID*(N) | Ampicillin |
B / 4 | pKan-PRFA1-9myc-AID*(N) | Ampicillin |
B / 5 | pHyg-PCUP1-AID*(N) | Ampicillin |
B / 6 | YIp204-PADH1-atTIR1-9myc | Ampicillin |
Kit Plate Map - #1000000120
Additional Required Plasmids
Plasmids pRS303-PADH1-AFB2 and YIp204-PADH1-AFB2 from the Ulrich Lab may also be required for some experiments. These plasmids are not included in the kit and have to be ordered separately.